Carafate - 58914-170-14 - (Sucralfate)

Alphabetical Index


Drug Information of Carafate

Product NDC: 58914-170
Proprietary Name: Carafate
Non Proprietary Name: Sucralfate
Active Ingredient(s): 1    g/10mL & nbsp;   Sucralfate
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Carafate

Product NDC: 58914-170
Labeler Name: Aptalis Pharma Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019183
Marketing Category: NDA
Start Marketing Date: 19931216

Package Information of Carafate

Package NDC: 58914-170-14
Package Description: 414 mL in 1 BOTTLE (58914-170-14)

NDC Information of Carafate

NDC Code 58914-170-14
Proprietary Name Carafate
Package Description 414 mL in 1 BOTTLE (58914-170-14)
Product NDC 58914-170
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sucralfate
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 19931216
Marketing Category Name NDA
Labeler Name Aptalis Pharma Inc.
Substance Name SUCRALFATE
Strength Number 1
Strength Unit g/10mL
Pharmaceutical Classes Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient]

Complete Information of Carafate


General Information